招聘内容:
招聘职位：临床研究员协调员—（兼职）重庆
工作地点：三级甲等医院
工作时间：一天（工作日）8:00~17:00 2012年3月~12月底
有兴趣的同学可以把简历投到：hr@
公司简介：
Chelsea Clinical Research is a Shanghai-based Contract Research Organization (CRO) which provides a comprehensive range of clinical trial services to international pharmaceutical companies, biotechnology companies and research institutions in China.
Our mission is to deliver service excellence and timely, quality results for our clients. As a professional drug development organization, we believe in the value of building trusted partnership with our clients.
职位要求：
- Bachelor or above Degree in medicine, pharmacy science or nursing;
- More than 1 year clinical monitoring experience in global oncology studies according to SFDA/ICH GCP;
- Self-motivated, interested in the clinical research work;
- Excellent interpersonal skills, negotiation skills and presentation skills;
- Good communication skills with fluent verbal and written English and Chinese;
- Willing to work at sites and can travel frequently;
- Teamwork spirit;
- Can work under pressure.
- More than 1 year clinical monitoring experience in global oncology studies according to SFDA/ICH GCP;
- Self-motivated, interested in the clinical research work;
- Excellent interpersonal skills, negotiation skills and presentation skills;
- Good communication skills with fluent verbal and written English and Chinese;
- Willing to work at sites and can travel frequently;
- Teamwork spirit;
- Can work under pressure.
岗位职责：
- To assist the site investigator to deliver high quality patient data in accordance with ICH/SFDA-GCP and as required by the SOPs and study protocol;
- To participate in the recruitment and screening of research patients;
- To be responsible for use of computer applications and other technology to enhance the efficiency of the
workflow in study activities including data collection and query resolution;
- To collect, prepare and submit of regulatory documents as per required by the site EC;
- To attend site initiation meeting;
- To prepare the documents for study monitor site visits;
- To assist investigator in obtaining proper written consent from each study participant according to the requirement;
- To perform functions necessary for completion of protocols including scheduling, patient enrollment, medical histories, clinical assessments, laboratory-phlebotomy and processing, diagnostic studies, dispensing of
investigational medication and overall organization and logistics of study visits;
- To complete and correct case report forms ensuring accuracy of all records connected with each
research patients;
- To assist the investigator to report and record all adverse events according to GCP Guidelines and the
request of sponsor;
- To maintain accurate record of all study supplies including lab kits, medications and other items dispensed to
patients;
- To maintain close contact with sponsor concerning patient enrollment, scheduling, dosing/dispensing, abnormal
laboratory values and adverse events;
- To ensure a smooth communication through the studies between the site investigator and Project team. Provide weekly timesheet to sponsor project team members;
- To update the TMFs and ensure the accuracy and completeness of TMFs;
- To perform other duties as required.
- To participate in the recruitment and screening of research patients;
- To be responsible for use of computer applications and other technology to enhance the efficiency of the
workflow in study activities including data collection and query resolution;
- To collect, prepare and submit of regulatory documents as per required by the site EC;
- To attend site initiation meeting;
- To prepare the documents for study monitor site visits;
- To assist investigator in obtaining proper written consent from each study participant according to the requirement;
- To perform functions necessary for completion of protocols including scheduling, patient enrollment, medical histories, clinical assessments, laboratory-phlebotomy and processing, diagnostic studies, dispensing of
investigational medication and overall organization and logistics of study visits;
- To complete and correct case report forms ensuring accuracy of all records connected with each
research patients;
- To assist the investigator to report and record all adverse events according to GCP Guidelines and the
request of sponsor;
- To maintain accurate record of all study supplies including lab kits, medications and other items dispensed to
patients;
- To maintain close contact with sponsor concerning patient enrollment, scheduling, dosing/dispensing, abnormal
laboratory values and adverse events;
- To ensure a smooth communication through the studies between the site investigator and Project team. Provide weekly timesheet to sponsor project team members;
- To update the TMFs and ensure the accuracy and completeness of TMFs;
- To perform other duties as required.
